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Ahmed Koriesh, MD Neuro-Pathology Page | 8 Brain Tumors Pathological finding Tumor Pseudorosette Ependymoma, SEGA Rosenthal fibers Pilocytic astrocytoma Rosettes Medulloblastoma Wet Keratin Craniopharyngioma Psammoma bodies Meningioma Fried egg Oligodendroglioma Medulloblastoma - Kids, midline, Cerebellum, diffuse contrast enhancement - Can seed in CSF (drop mets) but rarely involve meninges - On MRS, there is a choline and taurine peak Stains positive for Synaptophysin Rosettes formation Pilocytic astrocytoma: - Kids, cystic with an enhancing mural nodule. - Can occur in optic tract in patients with NF1 - Associated with BRAF gene mutation Pathology: Cells with long processes - Rosenthal fibers (intense red deposits formed of hyaline) Hair like processes arranged in Rosenthal fiber Smear of pilocytic cells bundles, resemble mats of hair

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  • Ahmed Koriesh, MD

    Neuro-Pathology P a g e | 8

    Brain Tumors

    Pathological finding Tumor

    Pseudorosette Ependymoma, SEGA Rosenthal fibers Pilocytic astrocytoma Rosettes Medulloblastoma Wet Keratin Craniopharyngioma Psammoma bodies Meningioma Fried egg Oligodendroglioma

    Medulloblastoma - Kids, midline, Cerebellum, diffuse contrast enhancement

    - Can seed in CSF (drop mets) but rarely involve meninges

    - On MRS, there is a choline and taurine peak

    Stains positive for Synaptophysin

    Rosettes formation

    Pilocytic astrocytoma: - Kids, cystic with an enhancing mural nodule.

    - Can occur in optic tract in patients with NF1

    - Associated with BRAF gene mutation

    Pathology: Cells with long processes - Rosenthal fibers (intense red deposits formed of hyaline)

    Hair like processes arranged in Rosenthal fiber Smear of pilocytic cells

    bundles, resemble mats of hair

  • Ahmed Koriesh, MD

    Neuro-Pathology P a g e | 9

    SEGA: - In patients with TS (TSC1 in ch 9q34 and TSC2 in ch 16)

    Pathology: large polygonal cells with abundant eosinophilic cytoplasm, perivascular pseudo-

    rosettes

    GFAP H&E

    Oligodendroglioma: - Adults, lobar, associated with IDH mutation

    - Anaplastic (Grade III) associated with allelic loss at ch 1p and 19q

    Pathology shows rounded nuclei, prominent cytoplasm with clear halo (Fried egg)

    GFAB stain H&E

    Colloid cyst: - Usually arise in the 3rd ventricle close to the foramen of

    Monroe

    - MRI: isointense on T1, hyperintnse in T2

    Pathology shows simple cuboidal or columnar epithelium,

    full of proteinaceous material

  • Ahmed Koriesh, MD

    Neuro-Pathology P a g e | 10

    Ependymoma: - Usually arise in 4th ventricle (children) or spinal cord (adults)

    - Can seed through CSF

    Pathology: perivascular pseudo-rosettes (Ependymal cell processes directed towards vessel wall

    with formation of perivascular anuclear zones of GFAP+ fibrillary processes)

    Subependymoma: - Arise in 4th ventricle in adults, doesn’t enhance

    - Clusters of cells embedded in dense glial fibrillary background, there may be pseudorosette

    Hemangioblastoma: - Cystic cerebellar tumor in adults with nodule of blood vessels, can involve the spine in VHL

    Pathology: vacuolated cells and vascular structures (packed thin walled vessels and large

    neoplastic cells with pink to clear cytoplasm with fine vacuoles containing PAS+ lipid)

  • Ahmed Koriesh, MD

    Neuro-Pathology P a g e | 11

    Meningioma: Pathology shows: Psammoma bodies (laminated calcific concretions) and whorls formation (cells

    arranged in whorls)

    Meningothelial whorls Psammoma bodies in psammomatous meningioma

    Choroid plexus papilloma: - Arise in lateral ventricle in children, homogenous enhancement

    Pathology: papillary or villous architecture (single layer of epithelial cells

    overlying a fibrovascular core)

    Pituitary adenoma: - Rounded or polygonal cells, rounded nuclei, cytoplasm either

    chromophobic, acidophilic or basophilic according to hormone production

    Chromophobic GH Producing (acidophilic)

  • Ahmed Koriesh, MD

    Neuro-Pathology P a g e | 12

    Craniopharyngioma: - Supra-sellar tumor in children, usually

    calcified

    Pathology: Keratinocytes in spheres

    called “wet Keratin”.

    Rathke’s cleft cyst: - Supra-sellar cystic tumor, isointense, non-enhancing

    Pathology: cyst lined with ciliated

    columnar epithelium with goblet

    cells.

    Pictures from Radiopedia Picture from Medscape website

  • Ahmed Koriesh, MD

    Neuro-Pathology P a g e | 13

    Hypothalamic hamartoma - In children, causes gelastic seizures and precocious puberty

    - MRI: non-enhancing, isointense

    Pathology: hypocellular mass of mature glia and neurons

    Germinoma: - Suprasellar or pineal (most common pineal tumor)

    Pathology: small reactive lymphocytes and large neoplastic germ cells.

  • Ahmed Koriesh, MD

    Neuro-Pathology P a g e | 14

    Pineocytoma: - In Adults, low grade tumor, contrast enhancing

    Pathology: characterized by large anuclear areas called pineocytomous rosettes

    DNET: - Children or young adults

    - MRI: Cortical, soap bubble appearance in MRI, no enhancement

    Pictures from Radiopedia Non-enhancing

  • Ahmed Koriesh, MD

    Neuro-Pathology P a g e | 15

    CNS lymphoma: - MRI: homogenous enhancement, vasogenic edema in T2, diffusion restriction in DWI

    - Usually arise at the edge of the ventricle

    FLAIR T1+C

    Epidermoid cyst: - Caused by entrapment of ectodermal tissue in neural tube during development

    - MRI: CSF signal in T1/T2, heterogenous in FLAIR, restricted diffusion (unlike arachnoid)

    Pathology: cyst lined by squamous epithelium, filled with keratin and cholesterol.

    T1 + contrast T2 DWI